- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04753801
What Are the Ingredients for the Best Form of the Best Possible Self (BPS) Intervention? (BestBPS)
August 6, 2024 updated by: Philipps University Marburg Medical Center
What Are the Ingredients for the Best Form of the Best Possible Self (BPS) Intervention? Combining the BPS Intervention With Mindfulness
This study aims to determine the relevant 'ingredients' to make the best possible self (BPS) intervention most efficacious and test whether the BPS's efficacy can be enhanced by including mindfulness aspects.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The best possible self (BPS) intervention is a brief positive psychology intervention to increase a person's positive affect and optimism.
The BPS has been used in different forms (writing vs. imagining/visualizing vs. writing + imagining/visualizing the best possible self).
However, it remains unclear which 'ingredients' are necessary to let the BPS unfold its effects.
This online study aims to determine the relevant 'ingredients' to make the best possible self (BPS) intervention most efficacious.
Since mindfulness interventions have recently indicated promising effects on positive and negative affect, another goal of this study is to test whether the BPS's efficacy can be enhanced by including aspects of mindfulness.
Study Type
Interventional
Enrollment (Actual)
181
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Marburg, Germany, 35032
- Department of Clinical Psychology and Psychotherapy, Philipps-University Marburg
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- fluent in the German language
- access to a computer/tablet/smartphone with audio output/headphones
Exclusion Criteria:
- not willing to take part in an online-intervention (duration: 60 minutes)
- no access to a computer/tablet/smartphone with audio output/headphones
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Best Possible Self (writing only)
Participants are asked to think and write about their best possible future self (15 min).
|
All participants are asked to take some time to think and write about the respective intervention group's content.
In some groups (after the writing exercise (approx.
15min)), participants are also asked to imagine that content or engage in a mindfulness activity or recall task for about 5 minutes.
|
|
Experimental: Best Possible Self (writing+imagining)
Participants are asked to think and write about their best possible future self (15 min) and, then to imagine their positive future (5 min).
|
All participants are asked to take some time to think and write about the respective intervention group's content.
In some groups (after the writing exercise (approx.
15min)), participants are also asked to imagine that content or engage in a mindfulness activity or recall task for about 5 minutes.
|
|
Experimental: Best Possible Self (writing+mindfulness)
Participants are asked to think and write about their best possible future self (15 min) and subsequently engage in a brief mindfulness sequence (5 min).
|
All participants are asked to take some time to think and write about the respective intervention group's content.
In some groups (after the writing exercise (approx.
15min)), participants are also asked to imagine that content or engage in a mindfulness activity or recall task for about 5 minutes.
|
|
Experimental: Best Possible Self (writing+recall)
Participants are asked to think and write about their best possible future self (15 min) and subsequently engage in a brief recall imagination task about the past two days (5 min).
|
All participants are asked to take some time to think and write about the respective intervention group's content.
In some groups (after the writing exercise (approx.
15min)), participants are also asked to imagine that content or engage in a mindfulness activity or recall task for about 5 minutes.
|
|
Active Comparator: Writing about the past
Participants are asked to think and write about activities of the past two days (15 min).
|
All participants are asked to take some time to think and write about the respective intervention group's content.
In some groups (after the writing exercise (approx.
15min)), participants are also asked to imagine that content or engage in a mindfulness activity or recall task for about 5 minutes.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in emotions (PANAS)
Time Frame: Change from pre (baseline) to post scores (approx. 30 minutes later)
|
Change scores are calculated for positive and negative sum scores (post- minus pre-scores; pre-scores will be used as a covariate).
|
Change from pre (baseline) to post scores (approx. 30 minutes later)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in state optimism ratings
Time Frame: Change from pre (baseline) to post scores (approx. 30 minutes later)
|
State Optimism measure (SOM), 7 items (each item 1(strongly disagree)-5(strongly agree)).
Change scores are calculated for positive and negative sum scores (post- minus pre-scores; pre-scores will be used as a covariate).
|
Change from pre (baseline) to post scores (approx. 30 minutes later)
|
|
Change in emotional responses to imagery of neutral, pleasant and aversive narrative scripts
Time Frame: Change from pre (baseline) to post scores (approx. 30 minutes later)]
|
Nine narrative imagery scripts are used.
Scenes included three neutral, standard social threat and positive/reward events.
All scripts were developed according to the recommendations of Lang (1979).
Participants are asked to rate the vividness of imagery (1= not vivid at all, 9= very vivid), the wish to avoid imagery (1 = no wish to avoid , 9 = strong wish to avoid imagery), their experienced anxiety (1= no anxiety, 9=very strong anxiety), displeasure (1 = pleasant, 9 = unpleasant), and emotional arousal (1 = relaxed, 9 = aroused) during imagery on a 9-point rating scale.
Emotional responses are averaged per category.
|
Change from pre (baseline) to post scores (approx. 30 minutes later)]
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Winfried Rief, Prof., Philipps University Marburg Medical Center
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
February 1, 2021
Primary Completion (Actual)
March 27, 2021
Study Completion (Actual)
March 31, 2021
Study Registration Dates
First Submitted
February 9, 2021
First Submitted That Met QC Criteria
February 9, 2021
First Posted (Actual)
February 15, 2021
Study Record Updates
Last Update Posted (Actual)
August 7, 2024
Last Update Submitted That Met QC Criteria
August 6, 2024
Last Verified
August 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- BestBPS
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
IPD Plan Description
Individual patient data will be shared with researchers providing a relevant and methodologically sound proposal
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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